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Sample GSM5031711 Query DataSets for GSM5031711
Status Public on May 03, 2024
Title PC_SR_1
Sample type SRA
 
Source name Melanoma biopsy
Organism Homo sapiens
Characteristics treatment: BRAFi+MEKi
time: Before the starting of 1 cycle
tissue: Melanoma biopsy
gender: not collected
Extracted molecule total RNA
Extraction protocol RNA was quantified and mixed at 10ng/µl
For RNA-seq analysis, libraries were prepared according to manufacturer's instructions (QuantSeq 3' mRNA-Seq Library Prep Kit FWD for Illumina, Lexogen GmbH) starting from 250ng of total RNA.
The amplified fragmented cDNA of 300 bp in size were sequenced in single-end mode using the NovaSeq6000 (Illumina) with a read length of 100 bp
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina NovaSeq 6000
 
Data processing the reads were trimmed toremove adapter sequences and low-quality ends and reads mapping to contaminating sequences (e.g., ribosomal RNA, phIX control) were filtered-out.
Genome_build: Hg38
Supplementary_files_format_and_content: tab-delimited text files include raw counts for each Sample
 
Submission date Jan 22, 2021
Last update date May 06, 2024
Contact name Rossella De Cegli
E-mail(s) decegli@tigem.it
Phone 08119230692
Organization name Tigem
Street address Via Campi Flegrei 34
City Pozzuoli
ZIP/Postal code 80078
Country Italy
 
Platform ID GPL24676
Series (2)
GSE165337 Transcriptomic profile of melanoma clinical samples treated with BRAF and MEK- inhibitors
GSE165338 RNAseq and Small-RNAseq dataset to comprehensively study the miRNA expression profiling of drug-resistant melanoma patients and cell lines
Relations
BioSample SAMN17496825
SRA SRX9920572

Supplementary file Size Download File type/resource
GSM5031711_S273_20200619120606_1_unique_counts.txt.gz 113.0 Kb (ftp)(http) TXT
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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